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一种基于多金属离子编码纳米球刷作为示踪物的“信号开启”适体传感器,可用于同时检测氯霉素和多氯联苯。

A "signal-on'' aptasensor for simultaneous detection of chloramphenicol and polychlorinated biphenyls using multi-metal ions encoded nanospherical brushes as tracers.

机构信息

State Key Laboratory Base of Novel Functional Materials and Preparation Science, Faculty of Materials Science and Chemical Engineering, Ningbo University, Ningbo 315211, PR China.

State Key Laboratory Base of Novel Functional Materials and Preparation Science, Faculty of Materials Science and Chemical Engineering, Ningbo University, Ningbo 315211, PR China.

出版信息

Biosens Bioelectron. 2015 Dec 15;74:718-24. doi: 10.1016/j.bios.2015.07.024. Epub 2015 Jul 16.

Abstract

A "signal-on'' aptasensor was developed for simultaneous detection of chloramphenicols (CAP) and polychlorinated biphenyl-72 (PCB72) with a novel multi-metal ions encoded nanospherical brushes as nanotracers. To construct the assay, the respective aptamer of CAP and PCB72 labeled magnetic gold nanoparticles as capture probes (aptamer-MGPs), and their complementary single strand DNA (s-DNA) encoded metal ions (Cd(2+) and Pb(2+)) on nanospherical branched polyethylene imine brushes as tracers (s-DNA-MSPEIs), were simultaneously synthesized. After that, the capture probe and tracers were connected through a hybridization reaction between s-DNA and aptamers. In the presence of CAP and PCB72, the analytes could react with the aptamers on capture probes and release the tracers into supernatant after magnetic separation. The released tracers with metal ions (Cd(2+) and Pb(2+)) could be simultaneously detected through the square wave voltammetry (SWV) without acid dissolution, which can switch the signals of the biosensor to "on'' state. Under optimal conditions, the assay could detect CAP and PCB72 as low as 0.3 pg mL(-1) with the dynamitic range from 0.001 to 100 ng mL(-1) and exhibited excellent selectivity. More importantly, the strategy can be extended easily to other targets after changing the corresponding aptamers and other metal ions tracers, which provides a promising and facile approach in multiplex detection of ultra-trace level of pollutants in food safety without more complex separation and washing steps.

摘要

一种“信号开启”适体传感器被开发出来,用于同时检测氯霉素(CAP)和多氯联苯-72(PCB72),其方法是使用新型多金属离子编码纳米球刷作为纳米示踪剂。为了构建该测定法,将各自的 CAP 和 PCB72 适体标记为磁金纳米颗粒作为捕获探针(适体-MGPs),并将其互补单链 DNA(s-DNA)编码的金属离子(Cd(2+)和 Pb(2+))作为示踪剂(s-DNA-MSPEIs)在纳米支化聚乙烯亚胺刷上合成。然后,通过 s-DNA 和适体之间的杂交反应连接捕获探针和示踪剂。在存在 CAP 和 PCB72 的情况下,分析物可以与捕获探针上的适体反应,并在磁性分离后将示踪剂释放到上清液中。释放的带有金属离子(Cd(2+)和 Pb(2+))的示踪剂可以通过方波伏安法(SWV)进行同时检测,无需酸溶解,这可以将生物传感器的信号切换到“开启”状态。在最佳条件下,该测定法可以检测到低至 0.3 pg mL(-1) 的 CAP 和 PCB72,动态范围为 0.001 至 100 ng mL(-1),并且表现出优异的选择性。更重要的是,该策略可以通过改变相应的适体和其他金属离子示踪剂,轻松扩展到其他目标,为食品安全中超痕量污染物的多重检测提供了一种有前途和简单的方法,无需更复杂的分离和洗涤步骤。

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